Canonical Allele Identifier: CA1047982072
Gene: ITIH1 HGNC NCBI

Linked Data

dbSNP Id: rs1699217970
gnomAD v3: 3-52786906-C-G
gnomAD v4: 3-52786906-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52786906C>G , CM000665.2:g.52786906C>G GRCh38
NC_000003.11:g.52820922C>G , CM000665.1:g.52820922C>G GRCh37
NC_000003.10:g.52795962C>G NCBI36
NG_016005.1:g.14315C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000273283.7:c.1734-39C>G MANE Select ENSP00000273283.2:n.1734-39C>G
ENST00000273283.6:c.1734-39C>G ENSP00000273283.2:n.1734-39C>G
ENST00000428133.5:c.393-39C>G ENSP00000395836.1:n.393-39C>G
ENST00000537050.5:c.870-39C>G ENSP00000443847.1:n.870-39C>G
ENST00000628722.2:n.1589-39C>G
NM_001166434.2:c.1308-39C>G NP_001159906.1:n.1308-39C>G
NM_001166435.2:c.870-39C>G NP_001159907.1:n.870-39C>G
NM_001166436.2:c.870-39C>G NP_001159908.1:n.870-39C>G
NM_002215.3:c.1734-39C>G NP_002206.2:n.1734-39C>G
NM_002215.4:c.1734-39C>G MANE Select NP_002206.2:n.1734-39C>G
NM_001166434.3:c.1308-39C>G NP_001159906.1:n.1308-39C>G